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| Product | Description | |
|---|---|---|
| Kidney-targeted In Vivo Kit | Kidney-targeted in vivo transfection kit. Functionally tested in mice tissue-targeted delivery of siRNA and pDNA via IV,IP,IT administrations. Kit includes: In vivo delivery reagent. Transfection Enhancer reagent. Protocol for mice and rats. Uses: Transfection of DNA, RNA, protein and small molecules. Product ID: 5071. |  Nevada, Texas, USA |
| kievitone hydratase | The enzyme from Fusarium sp. hydrates the methylbutenyl sidechain of the isoflavonoid phytoalexins, thus reducing their toxicity. Group: Enzymes. Synonyms: KHase; kievitone-hydrate hydro-lyase. Enzyme Commission Number: EC 4.2.1.95. CAS No. 70431-10-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5079; kievitone hydratase; EC 4.2.1.95; 70431-10-6; KHase; kievitone-hydrate hydro-lyase. Cat No: EXWM-5079. |  |
| KIF18A-IN-1 | KIF18A-IN-1 is an inhibitor of the mitotic kinesin KIF18A with anti-tumor activity. KIF18A targeted inhibitors may activate mitotic checkpoints and selectively kill chromosomally unstable cancer cells[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2600559-12-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145034. |  |
| KIF18A-IN-6 | KIF18A-IN-6 (Compound 134) is an orally active KIF18A inhibitor with an IC50 of 0.016 ?M against KIF18A microtubule-dependent ATPase activity[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2914879-10-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-153065. | |
| Kifunensine | mannosidase inhibitor. Group: Fluorescence/luminescence spectroscopyenzyme activators, inhibitors & substrates. |  |
| Kifunensine | Kifunensine is an alkaloid produced by the fungus, Kitasatosporia kifunense. It is a potent inhibitor of the mannosidase I enzyme. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Kifunensine | Kifunensine, a potent and selective inhibitor of class I α-mannosidases isolated from Actinomycete, prevents α-mannosidases I from trimming mannose residues on glycoproteins. Kifunensine inhibits ERAD [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: FR-900494. CAS No. 109944-15-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19332. | |
| Kifunensine diacetonide | Kifunensine diacetonide. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Kigamicin A | Kigamicin A is produced by the strain of Amycolatopsis sp. ML-630-mFl. It showed activity against gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) with MIC of 0.025-0.78 μg/mL. Molecular formula: C34H35NO13. Mole weight: 665.64. |  |
| Kigamicin B | Kigamicin B is produced by the strain of Amycolatopsis sp. ML-630-mFl. It showed activity against gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) with MIC of 0.025-0.78 μg/mL. Molecular formula: C40H45NO15. Mole weight: 779.78. | |
| Kigamicin C | Selectively kills PANC-1 cells (a pancreatic cell line) at concentrations 100 times lower under nutrient starved conditions than in normal conditions; active in vivo against a human pancreatic cancer xenograft model; also inhibits the growth of gram positive bacteria including MRSA, but is not active against gram negative bacteria. Synonyms: (1S,3R,4S,8aR,11aR)-3-[[(2S,5S,6R)-5-[(2,6-dideoxy-3-O-methyl-b-D-arabinohexopyranosyl)oxy]tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-1,2,3,4,8a,9,11,11a,13,14-decahydro-1,4,17,18-tetrahydroxy-11a-methyl-oxazolo[3,2-b]xantheno[4',3',2':4,5][1,3]benzodioxino[7,6-g]isoquinoline-16,19-dione. Grade: >98% by HPLC. CAS No. 680571-51-1. Molecular formula: C41H47NO16. Mole weight: 809.81. | |
| Kigamicin C | Kigamicin C was discovered by an anti-austerity strategy targeting cancer cells' tolerance to starvation. It selectively kills PANC-1 cells (a pancreatic cell line) at concentrations 100 times lower under nutrient starved conditions than in normal conditions. The mechanism of action is proposed to be via blocking of the activation of PKB/Akt caused by the withdrawal of nutrients. Active in vivo against a human pancreatic cancer xenograft model. Also inhibits the growth of Gram-positive bacteria including Staphylococcus aureus MRSA, but not active against Gram-negative bacteria. Group: Biochemicals. Grades: Highly Purified. CAS No. 680571-51-1. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Kigamicin D | Kigamicin D is produced by the strain of Amycolatopsis sp. ML-630-mFl. It showed activity against gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) with MIC of 0.025-0.78 μg/mL. It also shows effect against L-1210 LB32T and other genera tumor cells with IC50 of 1 μg/mL. Synonyms: 1,2,3a,4,6,7,10,11,12,13-Decahydro-11-[[5-[[5-[(tetrahydro-5-hydroxy-4-methoxy-6-methyl-2H-pyran-2-yl)oxy]tetrahydro-4-methoxy-6-methyl-2H-pyran-2-yl]oxy]tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-10,13,15,16-tetrahydroxy-3a-methyl-7,8-(methylenedioxy)-17a-aza-3,9-dioxa-17aH-cyclopenta[b]hexaphene-14,17-dione. Molecular formula: C48H59NO19. Mole weight: 953.98. | |
| Kihadanin B | Kihadanin B is a citrus limonoid that can be purified from the peels of immature Citrus unshiu. Kihadanin B suppresses adipogenesis through repression of the Akt-FOXO1-PPARγ axis in 3T3-L1 adipocytes. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Powder. CAS No. 73793-68-7. Molecular formula: C26H30O9. Mole weight: 486.5. Purity: 0.98. Canonical SMILES: CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=CC(OC6=O)O)C)C)C. Product ID: ACM73793687. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Kijanimicin | Kijanimicin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: kijanimicin. Product Category: Heterocyclic Organic Compound. CAS No. 78798-08-0. Molecular formula: C67H100NO24. Mole weight: 1317.5099;g/mol. Purity: 0.96. IUPACName: From Actinomadura Kijaniata. Canonical SMILES: CC1CC(C(C2C1C3(C(C=C2)C(=CCC(C(=CC4C=C(C(CC45C(=O)C(=C3O)C(=O)O5)C)CO)C)OC6CC(C(C(O6)C)NC(=O)OC)(C)[N+](=O)[O-])C)C)OC7CC(C(C(O7)C)O)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC)O)OC1CC(C(C(O1)C)O)O)C. Density: 1.35g/cm³. Product ID: ACM78798080. Alfa Chemistry ISO 9001:2015 Certified. | |
| Kijanimicin | A tetronic acid related to saccharocarcin, chlorothricin, versipelostatin and tetrocarcin; contains an unusual nitroaminoglycoside; a potent antibacterial, antimalarial and antitumour active; inhibits transcription from the promoter of GRP78, a gene that is activated as part of a stress signalling pathway under glucose deprivation resulting in unfolded protein response (UPR). Synonyms: NSC 329515; Sch 25663. Grade: >99% by HPLC. CAS No. 78798-08-0. Molecular formula: C67H100N2O24. Mole weight: 1317.51. | |
| Kijanimicin (Antibiotic Sch 25663) | Kijanimicin is a tetronic acid related to saccharocarcin, chlorothricin, versipelostatin and tetrocarcin. Like the tetrocarcins, kijanimicin contains an unusual nitro-aminoglycoside. Kijanimicin is a potent antibacterial, antimalarial and antitumor activity. However, several members of this class have received considerable literature focus. Versipelostatin was shown to inhibit transcription from the promoter of GRP78, a gene that is activated as part of a stress signaling pathway under glucose deprivation resulting in unfolded protein response (UPR). The UPR-inhibitory action was seen only in conditions of glucose deprivation and caused selective and massive killing of the glucose-deprived cells. While tetrocarcin A appears to target the phosphatidylinositide-3'-kinase/Akt signaling pathway. Group: Biochemicals. Alternative Names: Antibiotic Sch 25663. Grades: Highly Purified. CAS No. 78798-08-0. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Kimcuongin | Kimcuongin is a coumarin isolated from Murraya paniculata leaves that has the potential to be used as a vasodilator. Synonyms: [1-(7-methoxy-2-oxochromen-8-yl)-3-methyl-1-oxobut-2-en-2-yl] 3-methylbut-2-enoate. Grade: 98.5%. CAS No. 1872403-23-0. Molecular formula: C20H20O6. Mole weight: 356.374. | |
| KIN1400 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| KIN1408 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| KIN-8194 | KIN-8194 is an orally active dual inhibitor of HCK and BTK, with IC50 values of 0.915 and <0.495 nM, respectively. KIN-8194 impairs growth and integrin-mediated adhesion of BTKi-resistant mantle cell lymphoma (MCL). KIN-8194 overcomes ibrutinib (HY-10997) resistance with a survival benefit in TMD-8 ABC DLBCL xenografted mice[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 330786-01-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15805. | |
| Kinamycin A | Kinamycin A is produced by the strain of Str. murayamaensis. Kinamycin A has antibacterial and mycobacterial effects, but it has weak activity against gram-negative bacteria. Synonyms: BRN 0505520; 2,3,4-Tri(acetyloxy)-1,2,3,4,6,11-hexahydro-1,7-dihydroxy-3-methyl-6,11-dioxo-5H-benzo(b)carbazole-5-nitrile; 1,2,3-Tris(acetyloxy)-11-diazonio-4,9-dihydroxy-2-methyl-10-oxo-2,3,4,10-tetrahydro-1H-benzo[b]fluoren-5-olate. Grade: >98%. CAS No. 35303-12-9. Molecular formula: C24H20N2O10. Mole weight: 496.42. | |
| Kinamycin B | Kinamycin B is produced by the strain of Str. murayamaensis. Kinamycin B has antibacterial and mycobacterial effects, but it has weak activity against gram-negative bacteria. Synonyms: BRN 0503790; (1R,2R,3R,4S)-2-acetyloxy-11-diazonio-1,3,4,10-tetrahydroxy-2-methyl-9-oxo-3,4-dihydro-1H-benzo[b]fluoren-5-olate. Grade: >98%. CAS No. 35303-13-0. Molecular formula: C20H16N2O8. Mole weight: 412.35. | |
| Kinase Inhibitor Library | A unique collection of 2230 kinase inhibitors for high throughput screening and high content screening for drug discovery in kinase related diseases; - Bioactivity and safety confirmed by pre-clinical research and clinical trials, and some of them are approved by FDA; - Targets include MAPK, PI3K, JAK, STAT, CDK, MEK, Insulin/IGF receptors, CaM Kinease II, PKA, JNK, PKC, RAF, EGFR, SAPK, GSK, MLCK, Src-family, IKK, PDGFR, VEGFR, etc; - Detailed compound information with structure, target, activity, IC50 value, and biological activity description; - Structurally diverse, medicinally active, and cell permeable; - NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L1600. Categories: Kinase Inhibitor Libraries. |  |
| Kinase(phosphorylating), protein, cPKC | Kinase(phosphorylating), protein, cPKC. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EC 2.7.1.37;PROTEIN KINASE, 3':5'-CYCLIC AMP DEPENDENT;PROTEIN KINASE C;PROTEIN KINASE C, RAT BRAIN;PROTEIN KINASE C, CALCIUM- AND LIPID-DEPENDENT;PKC;protein kinase C from rat brain;PROTEIN KINASE C FROM RAT BRAIN, 5 U/VIAL*. Product Category: Heterocyclic Organic Compound. CAS No. 141436-78-4. Product ID: ACM141436784. Alfa Chemistry ISO 9001:2015 Certified. | |
| Kinesin family member 27, isoform CRAb (84-103) | A peptide fragment of Kinesin family member 27, isoform CRAb. KIF27 plays an essential role in motile ciliogenesis. Synonyms: Kinesin-Like Protein KIF27 isoform CRA_b (84-103). | |
| Kinesin-like protein KIF20A (12-20) | Kinesin-like protein KIF20A (12-20) is a 9-aa peptide. Kinesin-like protein KIF20A is a mitotic kinesin required for chromosome passenger complex (CPC)-mediated cytokinesis. Synonyms: Mitotic kinesin-like protein 2 (12-20); Rab6-interacting kinesin-like protein (12-20). | |
| Kinesin-like protein KIF20A (284-293) | Kinesin-like protein KIF20A (284-293) is a 10-aa peptide. Kinesin-like protein KIF20A is a mitotic kinesin required for chromosome passenger complex (CPC)-mediated cytokinesis. Synonyms: Mitotic kinesin-like protein 2 (284-293); Rab6-interacting kinesin-like protein (284-293). | |
| Kinesin-like protein KIF20A (809-817) | Kinesin-like protein KIF20A (809-817) is a 9-aa peptide. Kinesin-like protein KIF20A is a mitotic kinesin required for chromosome passenger complex (CPC)-mediated cytokinesis. Synonyms: Mitotic kinesin-like protein 2 (809-817); Rab6-interacting kinesin-like protein (809-817). | |
| Kinesore | Kinesore is an inhibitor of the KLC2-SKIP Interaction. Uses: Scientific research. Group: Signaling pathways. CAS No. 363571-83-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-112777. | |
| Kinetensin | Kinetensin (human) is an endogenous neurotensin-like peptide originally isolated from pepsin-treated human plasma. It increases vascular permeability and releases histamine from rat mast cells. It induces histamine release from rat peritoneal mast cells with ED50 value of 10 mM in vitro. Synonyms: Kinetensin (human); Neurotensin-related peptide; H-Ile-Ala-Arg-Arg-His-Pro-Tyr-Phe-Leu-OH; L-isoleucyl-L-alanyl-L-arginyl-L-arginyl-L-histidyl-L-prolyl-L-tyrosyl-L-phenylalanyl-L-leucine. Grade: ≥95%. CAS No. 103131-69-7. Molecular formula: C56H85N17O11. Mole weight: 1172.38. | |
| Kinetin | Kinetin (N6-furfuryladenine) belongs to the family of N6-substituted adenine derivatives known as cytokinins, which are plant hormones involved in cell division, differentiation and other physiological processes. Kinetin has anti-aging effects [1]. Uses: Scientific research. Group: Natural products. Alternative Names: 6-Furfuryladenine; N6-Furfuryladenine. CAS No. 525-79-1. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g. Product ID: HY-N0160. | |
| Kinetin | Kinetin was the first cytokinin discovered. It is also adenine-based. Uses: Kinetin was the first cytokinin discovered based on its cell division promotion from a mixture of autoclaved herring sperm. kinetin like other cytokinins promotes cell division, shoot proliferation and organogenesis, aids in the maintenance of the shoot-apical meristem, disrupts apical dominance, and delays senescence. Additional or Alternative Names: 6-Furfurylaminopurine. Product Category: Heterocyclic Organic Compound. Appearance: White to Yellow Crystalline. CAS No. 525-79-1. Molecular formula: C10H9N5O. Mole weight: 215.21 g/mol. Product ID: ACM525791. Alfa Chemistry ISO 9001:2015 Certified. | |
| Kinetin | A cell division factor found in various plant parts and in yeast. A plant growth regulator. Augments growth of microbial cultures. Group: Biochemicals. Alternative Names: N-(2-Furanylmethyl)-. Grades: Highly Purified. CAS No. 525-79-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Kinetin 99+% (HPLC) | Kinetin 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| Kinetin riboside | Kinetin riboside, a cytokinin analog, can induce apoptosis in cancer cells. It inhibits the proliferation of HCT-15 cells with an IC50 of 2.5 ?M. Uses: Scientific research. Group: Signaling pathways. Alternative Names: N6-Furfuryladenosine. CAS No. 4338-47-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-101055. | |
| Kinetin Riboside (6-Furfurylaminopurine Riboside, N6-Furfuryladenosine) | Used as an anticancer and antiviral agent. Group: Biochemicals. Alternative Names: 6-Furfurylaminopurine Riboside, N6-Furfuryladenosine. Grades: Highly Purified. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Kininogen high molecular weight, Two Chain from human plasma | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Kininogen, low molecular weight from human plasma | ?95% (SDS-PAGE), lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| KINK-1 hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Kin of IRRE-like protein 3 isoform 2 precursor (402-419) | A peptide fragment of Kin of IRRE-like protein 3 isoform 2 precursor. Kin of IRRE-like protein 3 probably acts as a homophilic adhesion molecule that promotes trans-cellular interactions and stabilize mossy fiber filipodia contact and subsequent synapse formation. Synonyms: Kin of irregular chiasm-like protein 3 isoform 2 precursor (402-419). | |
| Kinsenoside | Kinsenoside is a main active component isolated from plants of the genus Anoectochilus, and exhibits many biological activities and pharmacological effects. Kinsenoside rescues the nucleus pulposus cells (NPCs) viability under oxidative stress and protects against apoptosis, senescence and mitochondrial dysfunction in a Nrf2-dependent way. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (4R)-4-(beta-D-Glucopyranosyloxy)dihydro-2(3H)-furanone. Product Category: Inhibitors. Appearance: Solid. CAS No. 151870-74-5. Molecular formula: C10H16O8. Mole weight: 264.23. Purity: 0.95. IUPACName: (4R)-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-one. Canonical SMILES: C1[C@H](COC1=O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O. Density: 1.59±0.1 g/ml. Product ID: ACM151870745. Alfa Chemistry ISO 9001:2015 Certified. | |
| Kinsenoside | Kinsenoside. Group: Biochemicals. Alternative Names: (+)-Kinsenoside. Grades: Plant Grade. CAS No. 151870-74-5. Pack Sizes: 25mg. Molecular Formula: C10H16O8, Molecular Weight: 264.228999999999. US Biological Life Sciences. | Worldwide |
| K ir1.1 Inhibitor, VU591 | The Kir1.1 Inhibitor, VU591 controls the biological activity of Kir1.1. This small molecule/inhibitor is primarily used for Neuroscience applications. Group: Fluorescence/luminescence spectroscopy. | |
| Kir1.1 Inhibitor, VU591 (Inward Rectifier Potassium Channel Kir1.1 Blocker, VU591) | A cell-permeable, benzoimidazole, renal outer medullary potassium channel (ROMK) blocker that selectively inhibits inward rectifier potassium channel, Kir1K.1 (IC50=240nM), in HEK-293 cells. At 10uM, it displays no effect on Kir2.1, Kir2.3, Kir4.1, and Kir7.1, with 150-fold selectivity over Kir6.2. In addition, it exhibits a modest off-target effect on the GABAA receptor (IC50=6.2uM) among a panel of cardiac and central nervous system ion channels and receptors. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Kir2.1 Inhibitor, ML133 - CAS 185669-79-8 | The Kir2.1 Inhibitor, ML133, also referenced under CAS 185669-79-8, controls the biological activity of Kir2.1. This small molecule/inhibitor is primarily used for Cancer applications. Group: Fluorescence/luminescence spectroscopy. | |
| Kir2.1 Inhibitor, ML133 (Inward Rectifier Potassium Channel Blocker, ML133) | A cell-permeable, renal outer medullary potassium (ROMK) blocker that is shown to inhibit inward rectifier potassium channel, Kir2.1 (IC50=1.8uM and 290nM, at pH 7.4 and pH 8.5, respectively). It exhibits little selectivity against other members of the Kir2.x family, but has no effect on Kir1.1 (IC50 >300uM) and displays weak activity for Kir4.1 and Kir7.1 (IC50=76uM and 33uM, respectively). It is reported to be assayed in 218 MLPCN HTS campaigns, demonstrating activity in only two assays that are not based on Kir2.1. Furthermore, it displays a relatively clean profile in a radioligand binding panel of 68 GPCRs, ion channels and transporters. Group: Biochemicals. Grades: Highly Purified. CAS No. 185669-79-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| KIRA6 | KIRA6 is an advanced small-molecule IRE1? RNase kinase inhibitor with an IC50 of 0.6 μM[2]. KIRA6 can trigger an apoptotic response[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1589527-65-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-19708. | |
| KIRA-7 | KIRA-7, an imidazopyrazine compound, binds the IRE1α kinase ( IC 50 of 110 nM) to allosterically inhibit its RNase activity. KIRA-7 has an anti-fibrotic effect [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1937235-76-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-124646. | |
| Kira8 | Kira8 (AMG-18) is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity with an IC 50 of 5.9 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMG-18. CAS No. 1630086-20-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-114368. | |
| Kirenol | Kirenol is isolated from Siegesbeckia orientalis with anti-inflammatory and analgesic activity[1]. Uses: Scientific research. Group: Natural products. CAS No. 52659-56-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg; 50 mg. Product ID: HY-N0559. | |
| Kirenol | Kirenol. Group: Biochemicals. Grades: Plant Grade. CAS No. 52659-56-0. Pack Sizes: 20mg. Molecular Formula: C20H34O4, Molecular Weight: 338.48. US Biological Life Sciences. | Worldwide |
| Kirromycin | Kirromycin is an antibiotic originally isolated from Streptomyces. It was shown to inhibit protein biosynthesis via acting on elongation factor Tu (EF-Tu). Synonyms: Mocimycin; Delvomycin. Grade: ≥95%. CAS No. 50935-71-2. Molecular formula: C43H60N2O12. Mole weight: 796.94. | |
| Kirromycin (Mocimycin, Delvomycin, MYC 8003, NSC 316094) | Antibiotic. Member of the elfermycin group. Antibacterial. Protein biosynthesis inhibitor. Specifically interacts with the bacterial elongation factor EF-Tu and prevents the release of EF-Tu from the bacterial ribosome after GTP hydrolysis. In the absence of ribosomes it induces EF-Tu-dependent hydrolysis of GTP. Animal growth promoter used in poultry breeding. Group: Biochemicals. Grades: Highly Purified. CAS No. 50935-71-2. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| Kirrothricin | Kirrothricin is originally isolated from Str. cinnamomeus Tu89. It has antibacterial action, but no activity to subtilis, Escherichia coli and fungi. Synonyms: 2H-Pyran-2-acetamide, N-((2E,4E,6S,7S,9S,10E,12E,14E,16E)-8,9-dihydroxy-6-methoxy-5,7,17-trimethyl-18-oxo-18-(1,2,5,6-tetrahydro-4-hydroxy-1-methyl-2-oxo-3-pyridinyl)-2,4-dihydroxy-5,5-dimethyl-6-((1E,3Z)-1,3-pentadienyl)-, (alphaS,2S,4S,6S)-. CAS No. 79190-00-4. Molecular formula: C44H64N2O10. Mole weight: 780.98. | |
| Kisspeptin-10 | Kisspeptin-10 is a potent endogenous ligand for the Kisspeptin receptor (KISS1, GPR54). Synonyms: Metastin (45-54); Kisspeptin-10 (human); KP-10; H-Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Phe-NH2; L-tyrosyl-L-asparagyl-L-tryptophyl-L-asparagyl-L-seryl-L-phenylalanyl-glycyl-L-leucyl-L-arginyl-L-phenylalaninamide. CAS No. 374675-21-5. Molecular formula: C63H83N17O14. Mole weight: 1302.4. | |
| Kisspeptin-10, human | Kisspeptin-10, human is a potent vasoconstrictor and inhibitor of angiogenesis. Kisspeptin-10, human acts as a tumor metastasis suppressor via its receptor GPR54. Kisspeptin-10-GPR54 system plays an important role in embryonic kidney development. Kisspeptin-10/GPR54 signaling induces osteoblast differentiation via NFATc4-mediated BMP2 expression [1]. Uses: Scientific research. Group: Peptides. CAS No. 374675-21-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P0254. | |
| Kisspeptin-10, rat | Kisspeptin-10, rat is a potent endogenous ligand for the Kisspeptin receptor (KISS1, GPR54). Synonyms: Kisspeptin-10 rat; Kisspeptin-10 (rat); Kisspeptin-10 (mouse, rat); H-Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Tyr-NH2. CAS No. 478507-53-8. Molecular formula: C63H83N17O15. Mole weight: 1318.4. | |
| Kisspeptin 234 TFA | Kisspeptin 234 TFA, is a 10 amino acid peptide as well as a kisspeptin receptor (KISS1, GPR54) antagonist. Kisspeptin 234 TFA is an analog of Kisspeptin 10 [1]. Uses: Scientific research. Group: Peptides. CAS No. 1848962-29-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1196A. | |
| Kisspeptin-54(human) | Kisspeptin-54(human) (Metastin(human)) is an endogenous ligand for kisspeptin receptor (KISS1, GPR54). Kisspeptin-54(human) binds to rat and human GPR54 receptors with K i values of 1.81 nM and 1.45 nM, respectively. Kisspeptin-54(human) inhibits tumor metastasis and stimulates the secretion of gonadotropin (LH) and testosterone [1] [2] [3] [4] [5] [6] [7] [8]. Uses: Scientific research. Group: Peptides. Alternative Names: Metastin(human). CAS No. 374683-24-6. Pack Sizes: 100 μg; 500 μg; 1 mg. Product ID: HY-P1022. | |
| Kistamicin A | Kistamicin A is produced by the strain of Microtetraspora parvasata subsp. kistna. It has antiviral effect, and its ID50 (μg/mL) against influenza virus MDCK cells and herpes simplex virus are respectively 3.6 and 44. It also has anti-gram-positive bacterial effects. Synonyms: Kistamycin A. CAS No. 155683-50-4. Molecular formula: C61H51ClN8O15. Mole weight: 1171.55. | |
| Kistamicin B | Kistamicin B is produced by the strain of Microtetraspora parvasata subsp. kistna. It has antiviral effect, and its ID50 (μg/mL) against influenza virus MDCK cells and herpes simplex virus are respectively 1.8 and 30. Synonyms: Kistamycin B. CAS No. 155683-51-5. Molecular formula: C70H60ClN9O16. Mole weight: 1318.73. | |
| KIT-6 | KIT-6. Group: Kit-6. CAS No. 12173-28-3. Pack Sizes: 10 g. |  |
| Kita-kyushu lung cancer antigen 1 (76-84) | Kita-kyushu lung cancer antigen 1 (76-84) is a bioactive peptide of Kita-kyushu lung cancer antigen 1. The tumor-associated antigen Kita-Kyushu lung cancer antigen-1 has been reported as not being expressed in normal tissues, except for the testis, and in the setting of non-small cell lung cancer. Synonyms: KK-LC-1 (76-84); Cancer/Testis Antigen 83 (76-84). | |
| Kitamycin A | It is originally isolated from Strptomyces sp. K385. Kitamycin A can inhibit the activity of plant growth. Molecular formula: C23H32N2O8. Mole weight: 464.51. | |
| Kit for Creating Hydrophilic PDMS Surface | Kit for Creating Hydrophilic PDMS Surface. Group: Self assembly and lithography. | |
| Kiwifruit concentrate powder | Kiwifruit concentrate powder contains a naturally potent proteolytic enzyme, actinidin, which enhances protein digestion. In-vitro studies have shown that actinidin enhances the digestion of a number of different food proteins, including soy, red meat, milk, gluten and gliaden. Kiwifruit concentrate powder may also help to improve gut motility, which is an important contributor to improved bowel function. The active enzyme content of Kiwifruit concentrate powder is protected by specialised pre-processing and freeze drying techniques which maintain optimal temperature and pH conditions. Group: Others. Activity: >20,000 u/g. Appearance: green to brown powder. Form: Freeze dried powder. Source: green kiwifruit. Actinidin; Kiwifruit concentrate powder; Kiwifruit powder. Cat No: KCP-001. | |
| Kiwi Powder | Kiwi fruit powder is made from fresh kiwi (Actinidia Chinensis), adopt the advanced spray drying technology. Kiwi juice powder is a rich source of vitamin C and vitamin A. Kiwi fruit powder can be used for drinks, health care products, baby food, puffed food, baking food, ice cream, and oatmeal. Group: Others. Kiwi Powder; Actinidia chinensis. Cat No: EXTC-083. | |
| Kjeldahl Nitrogen, Total (TKN) - WS | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). | |
| KJ Pyr 9 | KJ Pyr 9 is an inhibitor of MYC with a Kd of 6.5 nM in in vitro assay. Uses: Scientific research. Group: Signaling pathways. CAS No. 581073-80-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-19735. | |
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